Canonical Allele Identifier: CA358785012

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178363418T>C (hg19) ; chr4:g.177442264T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177442264T>C , CM000666.2:g.177442264T>C	GRCh38
NC_000004.11:g.178363418T>C , CM000666.1:g.178363418T>C	GRCh37
NC_000004.10:g.178600412T>C	NCBI36
NG_011845.2:g.5240A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.112A>G MANE Select	ENSP00000264595.2:p.Asn38Asp
ENST00000264595.6:c.112A>G	ENSP00000264595.2:p.Asn38Asp
ENST00000506853.5:n.146A>G
ENST00000510955.5:n.146A>G
ENST00000511231.1:n.146A>G
NM_000027.3:c.112A>G	NP_000018.2:p.Asn38Asp
NM_001171988.1:c.112A>G	NP_001165459.1:p.Asn38Asp
NR_033655.1:n.240A>G
XM_006714123.2:c.112A>G	XP_006714186.1:p.Asn38Asp
XR_001741155.2:n.206A>G
NM_000027.4:c.112A>G MANE Select	NP_000018.2:p.Asn38Asp
NM_001171988.2:c.112A>G	NP_001165459.1:p.Asn38Asp
NR_033655.2:n.174A>G